Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review

BackgroundMutations of the Wilms tumor suppressor-1 gene (WT1) are associated with life-threatening glomerulopathy, disorders of sexual development, Wilm's tumor, and gonadal malignancies. Our objectives were to describe the clinical presentations, age of progression, and onset of complications...

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Detalhes bibliográficos
Main Authors: Patricia Arroyo-Parejo Drayer, Wacharee Seeherunvong, Chryso P. Katsoufis, Marissa J. DeFreitas, Tossaporn Seeherunvong, Jayanthi Chandar, Carolyn L. Abitbol
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2022-04-01
Colecção:Frontiers in Pediatrics
Assuntos:
Wilms tumor
congenital nephrotic syndrome
steroid-resistant nephrotic syndrome
46XY sex reversal
disorders of sexual development
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fped.2022.847295/full
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